Canonical Allele Identifier: PA1139689366
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 970439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Leu475His
CA8313825
NM_000080.4:c.1424T>A